ENST00000321612.8:c.2159A=
MANE Select
|
ENSP00000370737.4:p.His720=
|
|
ENST00000638233.1:n.594A=
|
|
|
ENST00000638661.1:c.359A=
|
ENSP00000491369.1:p.His120=
|
|
ENST00000638694.1:n.346A=
|
|
|
ENST00000639318.1:c.359A=
|
ENSP00000491932.1:p.His120=
|
|
ENST00000639364.1:n.1859A=
|
|
|
ENST00000639443.1:n.1727A=
|
|
|
ENST00000639954.1:n.1867A=
|
|
|
ENST00000640505.1:n.398A=
|
|
|
ENST00000321612.6:c.2159A=
|
ENSP00000370737.3:p.His720=
|
|
NM_000170.2:c.2159A= , LRG_643t1:c.2159A=
|
NP_000161.2:p.His720=
|
|
NM_000170.3:c.2159A=
MANE Select
|
NP_000161.2:p.His720=
|
|